HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl ester → N-Phenylpiperidine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl ester | HCID 58737530 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Phenylpiperidine-3-carboxamide | HCID 16227111 | 99% |
Reaction Steps
A solution of 3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl ester (1.80 mol, 608 mg) and Pd—C 30% (100 mg) in CH3OH (10 mL) at 25° C. were added to a Paar hydrogenator low pressure reaction vessel. The mixture was reacted at 55 psi with vigorous shaking until hydrogen uptake subsided (2 h). The catalyst was filtered through a pad of celite. The filtrate was concentrated in vacuo which provided piperidine-3-carboxylic acid phenylamide (367 mg, 367 mg theoretical, 99%) as a white foam: LRMS m/z 205 (M++1, C12H16N2O requires 205).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132551B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-1a8ff64acd2145aa85ccbaaf1f77f85a |
| Source note | uspto-grants-2006_11 |